Clearance Summary
POWDER FREE VINYL EXAMINATION GLOVE received FDA 510(k) clearance under submission number K032071, sponsored by Shanghai Foremost Plastic Industrial Co., Ltd.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2003-10-10.
- Submission: K032071
- Applicant / Sponsor: Shanghai Foremost Plastic Industrial Co., Ltd.
- Clearance pathway: Abbreviated
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 2003-10-10
Classification & Regulation
This clearance is catalogued under FDA product code LYZ and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.